Team:Bielefeld-CeBiTec/Results/CO2-fixation/RuBisCO
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It was our approach to enable carbon fixation in <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Organisms#E.coli" target="_blank"><i>E. coli</i></a> for generating an autotrophic organism. Implemention of the calvin cycle in the heterotrophic model organism <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Organisms#E.coli" target="_blank"><i>E. coli</i></a> should be associated by expression of the carboxysome, to generate a higher efficiency. | It was our approach to enable carbon fixation in <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Organisms#E.coli" target="_blank"><i>E. coli</i></a> for generating an autotrophic organism. Implemention of the calvin cycle in the heterotrophic model organism <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Organisms#E.coli" target="_blank"><i>E. coli</i></a> should be associated by expression of the carboxysome, to generate a higher efficiency. | ||
- | As a carbon source for our experimtens with <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Organisms#E.coli" target="_blank"><i>E. coli</i></a>, we choose a pentose, Xylose. Thereby could be ensured, that the glycolysis for the generation of energy could be avoid. Xylose is metabolized by the cells to ribulose-5-phosphate. This is the substrate for the phosphoribulokinase A from <i> | + | As a carbon source for our experimtens with <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Organisms#E.coli" target="_blank"><i>E. coli</i></a>, we choose a pentose, Xylose. Thereby could be ensured, that the glycolysis for the generation of energy could be avoid. Xylose is metabolized by the cells to ribulose-5-phosphate. This is the substrate for the phosphoribulokinase A from <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Organisms#E.coli" target="_blank"><i>E. coli</i></a>, which is recombinant expressed in <a href="https://2014.igem.org/Team:Bielefeld-CeBiTec/Notebook/Organisms#S.elongatus" target="_blank"><i>Snyechoccous elongatus</i></a>, because it naturally dos not occur. The prkA attaches a phosphate group to ribulose-5-phosphate generating ribulose-1,5-bisphophate. This again is used by the RuBisCO, producing 3-phosphoglycerate. This is then used in the last reactions of the glycolysis and is metabolized to pyruvate. This can be used by the cells in the central metabolism. The reaction mechanism is illustrated in figure 1. |
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<a href="https://static.igem.org/mediawiki/2014/5/54/https://static.igem.org/mediawiki/2014/3/3b/Bielefeld-CeBiTec_2014-10-15_Xylose_pathway.png" target="_blank"><img src="https://static.igem.org/mediawiki/2014/3/3b/Bielefeld-CeBiTec_2014-10-15_Xylose_pathway.png" width="450px"></a><br> | <a href="https://static.igem.org/mediawiki/2014/5/54/https://static.igem.org/mediawiki/2014/3/3b/Bielefeld-CeBiTec_2014-10-15_Xylose_pathway.png" target="_blank"><img src="https://static.igem.org/mediawiki/2014/3/3b/Bielefeld-CeBiTec_2014-10-15_Xylose_pathway.png" width="450px"></a><br> | ||
- | <font size="2" style="text-align:center;"><b> | + | <font size="2" style="text-align:center;"><b>Figure 1:</b> Pathway of the D-xylose consumption in <i>E. coli</i> for the fixation of carbon dioxide by the RuBisCO from <i>Halothiobacillus neapolitnaus</i>. For this approach the substrate ribulose 1,5-bisphosphate needs to be accumulated in the cell. This is realzied be the PrkA from <i>Snyechoccous elongatus</i>.</font> |
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Revision as of 16:56, 17 October 2014
Module II - Carbon Dioxide (CO2) Fixation
Introduction
The Ribulose 1,5-bisphosphate Carboxylase Oxygenase (RuBisCO) is the most important enzyme in the Calvin cycle. It binds gaseous carbon dioxide to ribulose-1,5-bisphosphate (Ru-BP) generating two molecules of 3-phosphoglycerate (3-PGA). Therefore it is responsible for the fixation of carbon dioxide. 3-PGA is further converted in the Calvin cycle to glycerinaldehyde-3-phosphate. This is an essential intermediate in the central metabolism, as it plays a central role in glycolysis and gluconeogenesis. RuBisCO enzymes are chracterised as enzymes with slow reaction rates with a kcat of approximately 20. Furthermore they catalyse a side reaction with oxygen instead of of carbon dioxide, deteriorating the catalytic efficiency. The inclusion of the RuBisCO in a carboxysome, would significantly improve the efficiency of carbon fixation.
It was our approach to enable carbon fixation in E. coli for generating an autotrophic organism. Implemention of the calvin cycle in the heterotrophic model organism E. coli should be associated by expression of the carboxysome, to generate a higher efficiency.
As a carbon source for our experimtens with E. coli, we choose a pentose, Xylose. Thereby could be ensured, that the glycolysis for the generation of energy could be avoid. Xylose is metabolized by the cells to ribulose-5-phosphate. This is the substrate for the phosphoribulokinase A from E. coli, which is recombinant expressed in Snyechoccous elongatus, because it naturally dos not occur. The prkA attaches a phosphate group to ribulose-5-phosphate generating ribulose-1,5-bisphophate. This again is used by the RuBisCO, producing 3-phosphoglycerate. This is then used in the last reactions of the glycolysis and is metabolized to pyruvate. This can be used by the cells in the central metabolism. The reaction mechanism is illustrated in figure 1.
Thin Layer Chromatography
Cultivation
Bild Carbonat-Gleichgewicht
Bild Reaktor Schema
Bild Reaktor
Kalbriergerade
Kultivierung